Canonical Allele Identifier: PA2827293477
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 217705
ClinVar RCV Id: RCV000201742 RCV000595708 RCV001053459 RCV001814113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317214.1:p.Arg12Cys
CA277803
NM_001330285.2:c.34C>T